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Essential diagnostics for lung health in medical research and clinical care. Concept Pulmonary Function Tests, Chest X-ray, CT Scan, Bronchoscopy, Blood Gas Analysis
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Tuberculosis (TB) has risen once again, as of 2023, to return to being the world’s deadliest infectious disease. TB causes around one million deaths annually, leaving devastating impacts on patients and their communities.1 Historically, TB has been treated in separate TB clinics worldwide that are independent under public health systems, generally isolated from standard primary-care clinics. In […]

Interstitial Lung Disease

An Introduction to Interstitial Lung Disease

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The MHRA has approved nerandomilast for the treatment of adults with idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF). Nerandomilast is an oral, preferential phosphodiesterase 4B (PDE4B) inhibitor with immunomodulatory and antifibrotic effects. The approval was supported by positive phase 3 FIBRONEER trial data demonstrating a slower decline in lung function compared with placebo.

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With multiple national and international meetings taking place throughout the year, deciding which conferences to attend isn't always straightforward. While scientific programs are an important consideration, opportunities for networking, collaboration, career development and practical learning can be just as valuable. To help identify the meetings making the biggest impact across respiratory and pulmonary medicine and related specialties, we asked members of the touchRESPIRATORY community their non-negotiable conferences and what makes them worth attending.

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Join us as leading experts discuss key data and perspectives from ATS 2026 The American Thoracic Society (ATS) 2026 International Conference brought together the latest research and clinical insights across respiratory medicine, highlighting advances in diagnosis, treatment and patient care. In this ...

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The American Thoracic Society’s annual conference was held in Orlando, Florida from May 15-20, bringing together global experts in pulmonary, critical care, and sleep medicine. Across the week, attendees shared new research and clinical advances through scientific sessions, abstract presentations, and collaborative discussions aimed at improving respiratory care and patient outcomes. In this interview, Dr Jean Elwing (University of Cincinnati, Cincinnati, OH, USA) breaks down the key presentations, sessions and abstracts from the conference, highlighting the substantial progress made in the field and the challenges that still remain

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Respirology Reflections is our new, expert-led, practice pearls series delivering concise, actionable insights from leading experts in respiratory and pulmonary medicine. Designed to help healthcare professionals stay current, it highlights real-world challenges, emerging evidence, and actionable strategies to enhance clinical practice, strengthen decision-making, and build confidence in an increasingly complex and fast-evolving field.

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Interstitial lung disease (ILD) encompasses a heterogeneous group of disorders that pose significant challenges for clinical trial design, from patient selection to endpoint definition and global implementation. Despite advances in therapeutic development, translating trial findings into real-world benefit remains difficult, particularly when study populations and protocols do not fully reflect the complexity of routine clinical practice. As part of our Respirology Reflections series, Dr Tejaswini Kulkarni discusses practical strategies for designing more inclusive and pragmatic ILD trials, including patient selection, recruitment, endpoint choice, and aligning study protocols with real-world care.

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Fibrotic interstitial lung diseases (ILDs) remain difficult to treat due to their clinical heterogeneity, variable trajectories, and an increasingly complex therapeutic landscape. As part of our Respirology Reflections series, we spoke with Prof. Girish B. Nair to discuss early treatment initiation, selecting and sequencing antifibrotic or immunosuppressive therapies, evaluating response and duration, managing side effects, and addressing comorbidities and disease variability over time.

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The PROLIFIC Risk Score, a multi-biomarker blood test for idiopathic pulmonary fibrosis (IPF), recently reached a major milestone as the first IPF biomarker accepted into the FDA’s Biomarker Qualification Program. This achievement underscores its potential to improve patient stratification and prediction of disease progression. In this interview, PROLIFIC Chair Peter Schafer discusses how the Risk Score works, the unmet needs it addresses, and its path toward full FDA qualification.

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We are thrilled to welcome Dr Kulkarni to the touchREVIEWS in Respiratory & Pulmonary Diseases Editorial Board and look forward to her expertise, leadership and vision contributing to the continued growth and impact of the journal.

Translating innovation into practice: Highlights from CHEST 2025
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The CHEST 2025 annual meeting brought together pulmonary, critical care, and sleep medicine experts to share emerging science, clinical insights, and forward-looking innovations shaping respiratory care. Through focused conversations with leaders across the field, these interviews highlight practical, practice-ready insights that clinicians can bring directly to patient care.

Clinical trials in fibrotic ILDs: New therapeutic targets and the rise of precision medicine
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As the therapeutic landscape for fibrotic interstitial lung diseases (ILDs) continues to evolve, new trials are redefining targeted treatment and precision medicine approaches. In this Q&A, Dr Tejaswini Kulkarni discusses her CHEST 2025 presentation, highlighting emerging therapeutic targets, the role of biomarkers, recruitment challenges, and innovative trial designs shaping the future of fibrotic ILD research.

Celebrating 25 years of the Pulmonary Fibrosis Foundation: driving awareness, research, and support
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The Pulmonary Fibrosis Foundation (PFF) is marking a major milestone in 2025: 25 years of progress in improving the lives of those affected by pulmonary fibrosis (PF). Since its founding in 2000, PFF has become a leading voice in patient support, education, research funding, and advocacy. This September we are also taking part in PFF’s Pulmonary Fibrosis Awareness Month (PFAM), which is held yearly. Through this campaign, the PFF aims to raise national awareness of pulmonary fibrosis, educate the public and healthcare professionals, amplify patient and caregiver voices, and inspire action through advocacy and fundraising efforts.

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As touchRESPIRATORY approaches 10 years of providing education for busy respiratory specialists, we are looking to the future—and it certainly looks bright!

touchVisionary Voices
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Physician burnout is at a critical point. In this episode, Nicky speaks with Dr Alfred Atanda about why so many physicians are burning out and what can be done to change the trend. From personal experience to system-wide solutions, Dr Atanda shares valuable insights on improving physician well-being and building a more effective healthcare culture.

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What if your medical degree could launch more than a clinical career? In this candid and compelling read, Dr Jon Edelson shares his lessons for early-career clinicians ready to think beyond the bedside and explore the business of medicine.

touchVisionary Voices
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In this episode, we explore the future of continuing medical education (CME) with the team behind touchIME. Hannah Fisher and Matthew Goodwin share insights into global and US trends, the importance of patient inclusivity and how educational outcomes are evolving to better measure the direct impact of learning on clinical practice and patient care.

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Boehringer Ingelheim has announced that its investigational drug, nerandomilast (BI 1015550), has successfully met the primary endpoint in the phase III FIBRONEERâ„¢-ILD study. The trial assessed the absolute change from baseline in forced vital capacity (FVC) [mL] at Week 52 compared ...

Coverage from: Key congresses 2024

The unmet need for effective treatments for childhood interstitial lung diseases (ILDs) is significant, with no drugs currently approved for this vulnerable population—unlike in adult patients.

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